Evidence map›Paper›PMID 38637822›Full record

ArticleGenome medicine2024

The emergence of highly resistant and hypervirulent Klebsiella pneumoniae CC14 clone in a tertiary hospital over 8 years.

Sharif Hala, Mohammed Malaikah, Jiayi Huang, Wesam Bahitham, Omniya Fallatah, Samer Zakri, Chakkiath Paul Antony, Mohammed Alshehri, Raeece Naeem Ghazzali, Fathia Ben-Rached and 13 more

Open access · goldAbstract read
In one paragraph

Article in Genome medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 26 citations in OpenAlex.

  1. Emergence of carbapenem-resistant putative hypervirulentEmerging microbes & infections · 2026
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  13. GenusMicroorganisms · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 3 countries.

Sharif HalaPathogen Genomics Laboratory, Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology, 23955-6900, Jeddah, Makkah, Saudi Arabia.
Mohammed MalaikahPathogen Genomics Laboratory, Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology, 23955-6900, Jeddah, Makkah, Saudi Arabia.
Jiayi HuangLaboratory of Infectious Disease Epidemiology, Biological and Environmental Science and Engineering (BESE) Division, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Wesam BahithamKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Omniya FallatahKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Samer ZakriKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Chakkiath Paul AntonyPathogen Genomics Laboratory, Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology, 23955-6900, Jeddah, Makkah, Saudi Arabia.
Mohammed AlshehriKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Raeece Naeem GhazzaliPathogen Genomics Laboratory, Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology, 23955-6900, Jeddah, Makkah, Saudi Arabia.
Fathia Ben-RachedPathogen Genomics Laboratory, Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology, 23955-6900, Jeddah, Makkah, Saudi Arabia.
Abdullah AlsahafiKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Asim AlsaediKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Ghadeer AlAhmadiKing Faisal Specialist Hospital and Research Centre, Jeddah, Saudi Arabia.
Mai KaakiKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Meshari AlazmiKAUST Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Baraa AlhajHusseinKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Muhammad YaseenKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Hosam M ZowawiKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Majed F AlghoribiKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Abdulhakeem O AlthaqafiKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Abdulfattah Al-AmriKing Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Danesh MoradigaravandLaboratory of Infectious Disease Epidemiology, Biological and Environmental Science and Engineering (BESE) Division, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia. danesh.moradigaravand@kaust.edu.sa.ORCID 0000-0001-6652-5617
Arnab PainPathogen Genomics Laboratory, Biological and Environmental Sciences and Engineering, King Abdullah University of Science and Technology, 23955-6900, Jeddah, Makkah, Saudi Arabia. arnab.pain@kaust.edu.sa.
King Saud bin Abdulaziz University for Health Sciences · SAKing Abdullah University of Science and Technology · SAThe University of Queensland · AUHokkaido University · JPKing Faisal Specialist Hospital & Research Centre · SAUniversity of Ha'il · SA

Funding

KAUST BAS/1/1020-01-01KAUST BAS/1/1108-01-01
6 · The paper itself

Abstract

backgroundKlebsiella pneumoniae is a major bacterial and opportunistic human pathogen, increasingly recognized as a healthcare burden globally. The convergence of resistance and virulence in K. pneumoniae strains has led to the formation of hypervirulent and multidrug-resistant strains with dual risk, limiting treatment options. K. pneumoniae clones are known to emerge locally and spread globally. Therefore, an understanding of the dynamics and evolution of the emerging strains in hospitals is warranted to prevent future outbreaks.

methodsIn this study, we conducted an in-depth genomic analysis on a large-scale collection of 328 multidrug-resistant (MDR) K. pneumoniae strains recovered from 239 patients from a single major hospital in the western coastal city of Jeddah in Saudi Arabia from 2014 through 2022. We employed a broad range of phylogenetic and phylodynamic methods to understand the evolution of the predominant clones on epidemiological time scales, virulence and resistance determinants, and their dynamics. We also integrated the genomic data with detailed electronic health record (EHR) data for the patients to understand the clinical implications of the resistance and virulence of different strains.

resultsWe discovered a diverse population underlying the infections, with most strains belonging to Clonal Complex 14 (CC14) exhibiting dominance. Specifically, we observed the emergence and continuous expansion of strains belonging to the dominant ST2096 in the CC14 clade across hospital wards in recent years. These strains acquired resistance mutations against colistin and extended spectrum β-lactamase (ESBL) and carbapenemase genes, namely bla

conclusionsOverall, these results demonstrate the clinical significance of ST2096 clones and illustrate the rapid evolution of an emerging hypervirulent and MDR K. pneumoniae in a clinical setting.

Indexed as

KlebsiellaKlebsiella pneumoniaeAnti-Bacterial Agentsbeta-LactamasesHumansPhylogenyPlasmidsTertiary Care CentersAnti-Bacterial Agentsbeta-LactamasesAntimicrobial resistanceKlebsiella pneumoniaePrecision epidemiologyWhole-genome sequencing

Identifiers

PMID38637822
PMCPMC11025284
OpenAlexW4394932215

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.